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Vol. 19, Issue 3, 971-983, March 2008

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The Interaction of JRAB/MICAL-L2 with Rab8 and Rab13 Coordinates the Assembly of Tight Junctions and Adherens Junctions

Rie Yamamura^*,, Noriyuki Nishimura^*, Hiroyoshi Nakatsuji^*, Seiji Arase, and Takuya Sasaki^*

*Departments of Biochemistry and Dermatology, Institute of Health Biosciences, The University of Tokushima Graduate School, Tokushima 770-8503, Japan

Submitted June 11, 2007; Revised November 5, 2007; Accepted December 6, 2007
Monitoring Editor: Asma Nusrat

	ABSTRACT

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

 
The assembly of tight junctions (TJs) and adherens junctions (AJs) is regulated by the transport of integral TJ and AJ proteins to and/or from the plasma membrane (PM) and it is tightly coordinated in epithelial cells. We previously reported that Rab13 and a junctional Rab13-binding protein (JRAB)/molecule interacting with CasL-like 2 (MICAL-L2) mediated the endocytic recycling of an integral TJ protein occludin and the formation of functional TJs. Here, we investigated the role of Rab13 and JRAB/MICAL-L2 in the transport of other integral TJ and AJ proteins claudin-1 and E-cadherin to the PM by using a Ca²⁺-switch model. Although knockdown of Rab13 specifically suppressed claudin-1 and occludin but not E-cadherin transport, knockdown of JRAB/MICAL-L2 and expression of its Rab13-binding domain (JRAB/MICAL-L2-C) inhibited claudin-1, occludin, and E-cadherin transport. We then identified Rab8 as another JRAB/MICAL-L2-C-binding protein. Knockdown of Rab8 inhibited the Rab13-independent transport of E-cadherin to the PM. Rab8 and Rab13 competed with each other for the binding to JRAB/MICAL-L2 and functionally associated with JRAB/MICAL-L2 at the perinuclear recycling/storage compartments and PM, respectively. These results suggest that the interaction of JRAB/MICAL-L2 with Rab8 and Rab13 coordinates the assembly of AJs and TJs.

	INTRODUCTION

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

 
Tight junctions (TJs) and adherens junctions (AJs) are located at the apical end of the basolateral membrane of polarized epithelial cells. Epithelial polarization entails a complex interplay between the coordinated assembly of TJs and AJs, and several fundamental cellular processes. These include the activation of evolutionarily conserved polarity protein complexes, the reorganization of actin and microtubule cytoskeletons, the redistribution of organelles, and the polarization of membrane traffic. During a series of processes, epithelial cells first form spot-like primordial AJs at the tips of the initial cell–cell contacts, and they develop belt-like mature AJs. In parallel with the maturation of AJs, TJs are formed at the apical side of AJs (Yap et al., 1997; Vasioukhin et al., 2000; Nelson, 2003; Takai and Nakanishi, 2003). However, the molecular mechanism that coordinates the assembly of TJs and AJs remains to be clarified.

While AJs principally initiate and maintain cell–cell contacts, TJs seal the intercellular space and delineate the boundaries between the apical and basolateral membranes. Both TJs and AJs are composed of integral membrane proteins and plaque proteins associated with the cytosolic side of the plasma membrane. The principal integral TJ and AJ proteins are claudins and E-cadherin, which form homophilic interactions with the same family of proteins on an adjacent cell to form the characteristic structures of TJs and AJs, respectively (Takeichi, 1995; Yap et al., 1997; Tsukita et al., 2001). Additional integral TJ and AJ proteins include occludin, junctional adhesion molecules, and nectins (Takai and Nakanishi, 2003; Ebnet et al., 2004). These integral membrane proteins are linked to a number of TJ and AJ plaque proteins in the cytosol, including zonula occludens (ZO) proteins (ZO-1, ZO-2, and ZO-3) and catenins, which in turn bind the actin cytoskeleton. These TJ and AJ plaque proteins have multiple protein binding motifs, and they form an organizing platform for a variety of scaffolding, signaling, and membrane trafficking proteins (Gonzalez-Mariscal et al., 2003).

Accumulating evidence has revealed that the membrane trafficking of integral TJ and AJ proteins plays a key role in the assembly and maintenance of TJs and AJs (Ivanov et al., 2005). Among a number of membrane trafficking proteins identified, Rab family small G proteins are key regulators (Takai et al., 2001; Zerial and McBride, 2001; Pfeffer and Aivazian, 2004). More than 60 different Rab family members have been identified in mammalian cells, and each member recognizes distinct subsets of intracellular membranes. Rab proteins cycle between the "inactive" guanosine diphosphate (GDP)-bound and "active" guanosine triphosphate (GTP)-bound forms, and they also undergo a membrane insertion and extraction cycle, allowing both spatial and temporal control of their activity. GTP-bound Rab proteins interact with specific effector proteins, and together they act to translate the signal from one Rab protein to several diverse components of membrane trafficking. In epithelial cells, Rab8 and Rab13 are identified as AJ and TJ plaque proteins (Zahraoui et al., 1994; Lau and Mruk, 2003). While Rab8 localizes to the trans-Golgi network, recycling endosomes, vesicular and tubular structures in the cytosol, membrane protrusions, and plasma membrane (PM) in addition to AJs (Huber et al., 1993b; Lau and Mruk, 2003; Ang et al., 2004), Rab13 resides at perinuclear membrane structures, vesicular structures in the cytosol, and PM in addition to TJs (Zahraoui et al., 1994; Marzesco et al., 2002; Terai et al., 2006). Rab8 interacts with Rab8ip/germinal center kinase (GCK), JFC1/Slp1, and Optineurin in a GTP-dependent manner (Ren et al., 1996; Hattula and Peränen, 2000; Hattula et al., 2006), and it is implicated in multiple transport pathways, including the epithelial-specific adaptor protein complex AP-1B-dependent basolateral transport, the polarized membrane traffic to the dendritic membrane, the actin-dependent movement of melanosomes, the formation and destruction of membrane protrusions, and the cell–cell adhesion (Huber et al., 1993a; Ang et al., 2003; Powell and Temesvari, 2004; Chabrillat et al., 2005; Hattula et al., 2006). Rab13 also binds to protein kinase A (PKA), and it regulates the assembly of functional TJs, neurite outgrowth, and neuronal regeneration (Marzesco et al., 2002; Köhler et al., 2004; Di Giovanni et al., 2005). However, the exact transport routes regulated by Rab8 and Rab13 remain to be determined.

Claudins, occludin, and E-cadherin are transported to and from the PM by multiple exocytic and endocytic pathways. For their transport from the PM, three distinct endocytosis pathways—clathrin-dependent endocytosis, caveolin-dependent endocytosis, and macropinocytosis—are identified in different cellular contexts (Bryant and Stow, 2004; D'Souza-Schorey, 2005; Ivanov et al., 2005). Endocytosed claudins, occludin, and E-cadherin are also detected in multiple sites, including early endosome antigen (EEA)1-positive early endosomes, Rab11-positive recycling endosomes, Rab7-positive late endosomes, Rab13-positive vesicles, Syntaxin4-positive compartments, and Syntaxin3-positive vacuolar apical compartments (Le et al., 1999; Harhaj et al., 2002; Hopkins et al., 2003; Ivanov et al., 2004; Matsuda et al., 2004; Balzac et al., 2005; Bruewer et al., 2005; Morimoto et al., 2005; Utech et al., 2005). From these sites, claudins, occludin, and E-cadherin can be transported to the PM. Although a variety of regulatory molecules, including actin and microtubule cytoskeletons, myosin II, Rac1, Cdc42, ARF6, and Rab11 have been identified, the exact transport routes of claudins, occludin, and E-cadherin to and from the PM are not defined (Bryant and Stow, 2004; D'Souza-Schorey, 2005; Ivanov et al., 2005).

We previously reported that Rab13 regulated the endocytic recycling of occludin, and we identified a junctional Rab13-binding protein (JRAB)/molecule interacting with CasL-like 2 (MICAL-L2) as a novel Rab13 effector protein (Morimoto et al., 2005; Terai et al., 2006). Although JRAB/MICAL-L2 was originally identified as a MICAL-related cDNA (Terman et al., 2002), it also mediated the endocytic recycling of occludin and regulated the formation of functional TJs in epithelial cells (Terai et al., 2006). In the present study, we investigated the role of Rab13 and JRAB/MICAL-L2 in the transport of claudins and E-cadherin to the PM by using a well-established Ca²⁺-switch model (Kartenbeck et al., 1991). Although Rab13 specifically mediated claudin but not E-cadherin transport, JRAB/MICAL-L2 regulated both claudin and E-cadherin transport. We then identified Rab8 as an additional JRAB/MICAL-L2 effector protein that controlled the Rab13-independent transport of E-cadherin.

	MATERIALS AND METHODS

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

 
Plasmid Construction
The mammalian expression vectors pCI-neo-Myc-JRAB/MICAL-L2-F, pCI-neo-Myc-JRAB/MICAL-L2-C, pCI-neo-HA-Rab1A, pCI-neo-HA-Rab3B, pCI-neo-HA-Rab5A, and pCI-neo-HA-Rab13 were described previously (Yamamoto et al., 2003; Terai et al., 2006). Rab13 cDNA was cloned into the pGEX-6P-1, pCI-neo-Myc, and pCI-neo-FLAG vectors. JRAB/MICAL-L2-CC (amino acids 806-912) and JRAB/MICAL-L2-CT (amino acids 913-1009) cDNAs were generated by polymerase chain reaction (PCR) by using pCI-neo-Myc-JRAB/MICAL-L2-F as a template, and they were then cloned into the pCI-neo-Myc vector. Mouse Rab8A cDNA was amplified by PCR by using a yeast two-hybrid prey clone (pACT2-Rab8A) as a template, and then it was cloned into pCI-neo-HA, pCI-neo-Myc, and pCI-neo-FLAG vectors. Canine Rab4A, mouse Rab8B, mouse Rab10, and rat Rab11A cDNAs were isolated by reverse transcription (RT)-PCR from Madin-Darby canine kidney (MDCK) cells, NIH3T3 cells, MTD-1A cells, and rat brain, respectively, and then they were cloned into the pCI-neo-HA vector. cDNAs for mouse MICAL-1 (Q8VDP3, 1048 amino acids), mouse MICAL-3 (Q8CJ19, 864 amino acids), and mouse MICAL-L1 (Q8BGT6, 870 amino acids) were isolated by RT-PCR from mouse lung, mouse brain, and MTD-1A cells, respectively. Mouse MICAL-2 (Q8BML1, 960 amino acids) cDNA was generated by PCR by using the RIKEN FANTOM clone 5330438E18 (DNAFORM, Ibaraki, Japan) as a template. MICAL-1, MICAL-2, MICAL-3, and MICAL-L1 cDNAs were cloned into the pCI-neo-Myc and pCI-neo-HA vectors. All plasmids constructed in this study were sequenced using an ABI Prism 3100 Genetic Analyzer (Applied Biosystems, Foster City, CA).

Antibodies
Glutathione-S-transferase (GST) and N-terminal GST-tagged Rab13 (GST-Rab13) proteins were expressed from the pGEX-6P-1 (GE Healthcare, Piscataway, NJ) vector in Escherichia coli strain DH5 and purified by using glutathione-Sepharose beads (GE Healthcare) according to the manufacturer's instructions. Two milligrams of GST or GST–Rab13 protein were immobilized on HiTrap NHS-activated columns (GE Healthcare) according to the manufacturer's instructions. Two female Wistar rats were immunized with 100 µg of GST–Rab13 protein twice at 4-wk intervals, after which whole blood from the animals was collected. Crude immunoglobulin fractions were prepared by ammonium sulfate precipitation and passed through a GST-immobilized column to remove any anti-GST antibody. The anti-Rab13 polyclonal antibody was further purified on a GST–Rab13-immobilized column according to the manufacturer's instructions. The rat anti-JRAB/MICAL-L2 antibody was described previously (Terai et al., 2006). The rat anti-occludin (MOC37) antibody was the kind gift from Dr. S. Tsukita (Kyoto University, Kyoto, Japan). Rabbit anti-claudin-1 and rabbit anti-ZO-1 were purchased from Zymed Laboratories (San Francisco, CA); rat anti-E-cadherin was from Takara (Otsu, Japan); mouse anti-EEA1 and mouse anti-Rab8 were from BD Biosciences (San Jose, CA); mouse anti-Golgi 58K, mouse anti-β-actin, and mouse anti-FLAG (M2) were from Sigma-Aldrich (St. Louis, MO); mouse anti-mannose 6-phosphate receptor (M6PR) was from Affinity BioReagents (Golden, CO); mouse anti-Myc (9E10) was from American Type Culture Collection (Manassas, VA); mouse anti-hemagglutinin (HA) (12CA5) and rat anti-HA (3F10) were from Roche Diagnostics (Mannheim, Germany); and rabbit anti-green fluorescent protein (GFP) was from Invitrogen (Carlsbad, CA).

Cell Culture and Transfection
MDCK, MDCK I, and MTD-1A cells were kindly supplied by Dr. W. Birchmeier (Max Delbrueck Center for Molecular Medicine, Berlin, Germany), Dr. T. Tsukamoto (Kitano Hospital, Osaka, Japan), and Dr. S. Tsukita (Kyoto University, Kyoto, Japan), respectively. Baby hamster kidney (BHK) and NIH3T3 cells were obtained from American Type Culture Collection. MDCK, MTD-1A, and BHK cells were cultured in DMEM with 10% fetal bovine serum (FBS), and MDCK I cells were cultured in DMEM with 5% FBS. MDCK, MDCK I, MTD-1A, and BHK cells were transfected using a Nucleofector device (Amaxa, Köln, Germany) or with Lipofectamine 2000 transfection reagent (Invitrogen) according to the manufacturers' instructions.

Recombinant Adenovirus Infection
The recombinant adenovirus expressing enhanced green fluorescent protein (EGFP) and Myc-JRAB/MICAL-L2-C (Ad-EGFP and Ad-Myc-JRAB/MICAL-L2-C) was described previously (Terai et al., 2006). MTD-1A cells were infected with Ad-EGFP or Ad-Myc-JRAB/MICAL-L2-C at a multiplicity of infection of 100.

RNA Interference
The 21-mer small interfering RNA (siRNA) duplexes targeting canine Rab13 (XM_850035 [GenBank] ), mouse JRAB/MICAL-L2 (AB182579 [GenBank] ), canine Rab8A (NM_001003152), canine MICAL-1 (XM_539079 [GenBank] ), canine MICAL-L1 (XM_538381 [GenBank] ), and canine JRAB/MICAL-L2 (XM_547017 [GenBank] ) and the control nonsilencing siRNA duplexes were obtained from B-Bridge (Sunnyvale, CA), and they were transfected using a Nucleofector device (Amaxa) according to the manufacturer's instructions. The target sequences were as follows: canine Rab13 (#1, 5'-GAGGACAGCTTCAACAACA-3'; #2, 5'-GACAATAACTACTGCATAT-3'; and #3, 5'-GCGCCTGCTTCTAGGGAAC-3'), mouse JRAB/MICAL-L2 (#1, 5'-GGACAAACCCTGTGGTTCA-3'; #2, 5'-GGACGGTTCAGGAGGCAAA-3'; and #3, 5'-GGCTGAAGCCTGTGGATAA-3'), canine Rab8A (#1, 5'-CCATAGAGCTCGATGGCAA-3'; #2, 5'-GCAAGAGAATTAAGCTACA-3'; and #3, 5'-GGAATCAAGTTCATGGAGA-3'), canine MICAL-1 (5'-GTGGTGAACCAGCGAGATA-3'), canine MICAL-L1 (5'-GAGAGAAGGTGCTGATGCA-3'), and canine JRAB/MICAL-L2 (5'-GCAGCAACATCGTGGACGT-3').

Quantitative Real-Time RT-PCR
Total RNA from MDCK cells transfected with control RNA, MICAL-1 siRNA, MICAL-L1 siRNA, and JRAB/MICAL-L2 siRNA duplexes were isolated using BioRobot EZ1 with RNA Universal Tissue kit (QIAGEN, Valencia, CA) and reverse transcribed using QuantiTect Reverse Transcription kit (QIAGEN) according to the manufacturers' instructions. Real-time PCR analysis was performed with an ABI 7500 Real-Time PCR System (Applied Biosystems) by using FastStart Universal SYBR Green Master (Roche Diagnostics) according to the manufacturer's specifications. Each sample was analyzed in triplicates for each pair of primers. The relative expression of MICAL-1, MICAL-L1, and JRAB/MICAL-L2 to glyceraldehyde-3-phosphate dehydrogenase (GAPDH) was calculated by the relative standard curve method using Sequence Detection Software version 1.4 (Applied Biosystems). Primer sequences were as follows: canine MICAL-1 (forward, 5'-ACCAGGAAGGAGCCCTAAAG-3' and reverse, 5'-CTCCTGGAAGCGGATAAGTG-3'), canine MICAL-L1 (forward, 5'-CAAGATGTTGGAAGCCATGA-3' and reverse, 5'-TAGCAGCTTCAGCACCTTCA-3'), canine JRAB/MICAL-L2 (forward, 5'-CACCTCGTGCAGAGACACCT-3' and reverse: 5'-GTGCAGTGTGTTGGAGCACT-3'), and canine GAPDH (forward, 5'-TCAACGGATTTGGCCGTATTGG-3' and reverse: 5'-TGAAGGGGTCATTGATGGCG-3').

Ca²⁺-Switch Assay
Ca²⁺-switch assay was performed as described previously (Kartenbeck et al., 1991). Briefly, MTD-1A or MDCK cells were grown in DMEM with 10% FBS (normal Ca²⁺ ion medium [NCM]) and sequentially incubated in Ca²⁺-free minimal essential medium without FBS (low Ca²⁺ ion medium [LCM]) for 1 h and in LCM with 20 mM EGTA (for MTD-1A cells) or 5 mM EGTA (for MDCK cells) for 2 h to remove extracellular Ca²⁺. Cells were then incubated in NCM for varying periods and processed for immunofluorescence microscopy. Experiments in the presence of cycloheximide were performed by incubating MDCK cells sequentially with LCM, LCM containing 5 mM EGTA and 20 µM cycloheximide, and NCM containing 20 µM cycloheximide.

Transferrin Uptake
MDCK cells were cultured in serum-free DMEM for 1 h, incubated with 50 µg/ml Alexa 488-transferrin (Alexa-Tf; Invitrogen) for 1 h, and subjected to either a Ca²⁺-switch assay in the continuous presence of 50 µg/ml Alexa-Tf or immunofluorescence microscopy.

Immunofluorescence Microscopy
MDCK and MTD-1A cells were grown on glass coverslips and fixed with one of the following: –20°C methanol (for anti-claudin-1 antibody) on ice for 5 min, 1% formaldehyde (for anti-occludin antibody) in phosphate-buffered saline (PBS) at room temperature for 15 min, or 2% formaldehyde (for other antibodies) in PBS at room temperature for 15 min. After permeabilization with 0.2% Triton X-100 in PBS for 15 min and blocking with 5% goat serum in PBS for 60 min, cells were incubated with primary antibodies for 60 min and with Alexa 488-, or Alexa 594-conjugated secondary antibodies (Invitrogen) at room temperature for 60 min. For triple-labeling, anti-FLAG (M2) antibody was labeled with Pacific Blue by using a Zenon antibody labeling kit (Invitrogen). Fluorescent images were acquired using a Radiance 2000 confocal laser-scanning microscope (Bio-Rad, Hercules, CA) or a C1plus confocal laser-scanning microscope (Nikon, Tokyo, Japan).

Quantitation of Claudin-1, Occludin, and E-Cadherin Length
To quantify the mean length of claudin-1, occludin, and E-cadherin per cell, the fields were randomly selected from fluorescent images to contain >100 cells. Total length of claudin-1, occludin, and E-cadherin at cell–cell contact sites was measured using Lumina Vision 2.4 program (Mitani, Fukui, Japan), and the mean length per cell was calculated by total length/total cell number. Statistical analysis was performed using Student's t test.

Ratio of Colocalized Area
To calculate the ratio of colocalized area, the fields were selected from fluorescent images to contain >100 cells. The JRAB/MICAL-L2-E-cadherin and JRAB/MICAL-L2-occludin colocalized area at perinuclear recycling/storage compartment (PNC) and PM was measured using Lumina Vision 2.4 program (Mitani). Although the colocalized structures that positioned at cell–cell contact sites were defined as PM, all other colocalized structures were defined as PNC. Ratio was calculated by colocalized area at PNC/colocalized area at PM.

Measurement of Transepithelial Electrical Resistance (TER)
MDCK I cells (8 x 10⁴) transfected with control RNA, MICAL-1 siRNA, MICAL-L1 siRNA, or JRAB/MICAL-L2 siRNA were plated onto Transwell filters (polycarbonate membranes with 12-mm diameter and 0.4-µm pore size; Corning Life Sciences, Acton, MA) and grown in NCM for 72–96 h and subjected to a Ca²⁺-switch assay in which the incubation in LCM with 5 mM EGTA was shortened to 10 min. TER was measured directly in culture media at 6 and 12 h after restoring Ca²⁺ by using a Millicell-ERS epithelial voltohmmeter (Millipore, Billerica, MA). TER values were calculated by subtracting the background TER of blank filters and by multiplying the surface area of the filter.

Two-Hybrid Screening
JRAB/MICAL-L2-C was cloned into the yeast two-hybrid bait vector pGBDU-C1 (James et al., 1996). A mouse 11-d-old embryo cDNA library in the yeast two-hybrid prey vector pACT2 was purchased from Clontech (Palo Alto, CA). The yeast strain PJ69-4A (MATa trp1-901 leu2-3112 ura3-52 his3-200 gal4 gal80 GAL2-ADE2 LYS2::GAL1-HIS3 met2::GAL7-lacZ) was sequentially transformed with pGBDU-JRAB/MICAL-L2-C and the mouse 11-d-old embryo cDNA library. Two-hybrid screening was performed and evaluated as described previously (James et al., 1996).

Coimmunoprecipitation
BHK and MTD-1A cells were lysed with 25 mM Tris/HCl, pH 7.5, containing 0.5% 3-[(3-cholamidopropyl)dimethylammonio]propanesulfonate (CHAPS), 125 mM NaCl, 1 mM MgCl₂, 20 µg/ml (4-amidinophenyl)-methanesulfonyl fluoride, and 100 µM guanosine 5'-O-(3-thio)triphosphate (GTPS)/GDP at 4°C for 15 min. After removing a fraction of the lysates, the remaining lysates were immunoprecipitated with the indicated antibodies bound to protein G-Sepharose beads (GE Healthcare) and washed three times with 25 mM Tris/HCl, pH 7.5, containing 0.1% CHAPS, 300 mM NaCl, 1 mM MgCl₂, and 10 µM GTPS/GDP. The samples were prepared for Western blot analysis.

Western Blot
Proteins were separated by SDS-polyacrylamide gel electrophoresis, and proteins were transferred to polyvinylidene difluoride membranes. Membrane blocking and antibody dilutions were done in Block Ace (Dainippon Pharmaceutical, Osaka, Japan). Blots were developed by chemiluminescence using a horseradish peroxidase-coupled secondary antibody (Jackson ImmunoResearch Laboratories, West Grove, PA) and Immobilon Western Chemiluminescent Horseradish Peroxidase Substrate (Millipore).

	RESULTS

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

 
Rab13 Is Involved in the Transport of Claudin-1 and Occludin, but not E-Cadherin, to the PM
We previously reported that Rab13 and JRAB/MICAL-L2 specifically regulated the endocytic recycling of occludin and the assembly of functional TJs (Terai et al., 2006). Because claudins but not occludin are recognized as the primary integral TJ proteins and the simultaneous and/or orchestrated endocytosis of integral TJ and AJ proteins is observed in a variety of physiological and pathological conditions (Ivanov et al., 2005), the question has naturally arisen as to whether Rab13 and JRAB/MICAL-L2 also regulate the transport of claudins and E-cadherin to the PM. In the present study, we have used a well established Ca²⁺-switch model (Kartenbeck et al., 1991) to investigate the transport of claudins, occludin, and E-cadherin to the PM. MDCK or MTD-1A cells were first incubated in Ca²⁺-chelated medium to internalize claudins, occludin, and E-cadherin from the PM and to induce the disassembly of cell–cell junctions. Subsequently, they were cultured in physiological Ca²⁺ medium to transport claudins, occludin, and E-cadherin to the PM and to induce the synchronous assembly of cell–cell junctions. The localizations of claudin-1, occludin, and E-cadherin were then analyzed by immunofluorescence microscopy at 0, 2, 4, 6, and 24 h after the restoration of physiological Ca²⁺.

To examine the role of Rab13, we designed siRNAs against the canine Rab13 sequence (XM_850035 [GenBank] ), and we transfected them into MDCK cells. All Rab13 siRNAs suppressed the expression of Rab13 protein in MDCK cells, whereas a nonsilencing control RNA did not (Figure 1A). The most effective Rab13-3 siRNA was used in the present study. In MDCK cells transfected with control RNA or Rab13 siRNA, claudin-1, occludin, and E-cadherin internalized from the PM and accumulated intracellularly after Ca²⁺ removal, and each was then transported to the PM within 24 h of Ca²⁺ restoration (Supplemental Figure S1, A–C). However, the kinetics of the transport of claudin-1 and occludin to the PM seemed different. In accordance with previous reports using a GTP hydrolysis-defective mutant of Rab13 (Rab13 Q67L) (Marzesco et al., 2002; Terai et al., 2006), the depletion of Rab13 slowed the kinetics of claudin-1 and occludin transport to the PM at 2, 4, and 6 h after Ca²⁺ restoration (Figure 1, B and C). In marked contrast, the disappearance of the intracellular staining of and/or the appearance of continuous PM staining of E-cadherin was indistinguishable between Rab13-depleted and control cells at 2 and 4 h after Ca²⁺ restoration (Figure 1D). These results demonstrated that Rab13 was specifically required for the transport of claudin-1 and occludin, but not E-cadherin, to the PM.

View larger version (60K): [in this window] [in a new window]   Figure 1. Rab13 is involved in the transport of claudin-1 and occludin, but not E-cadherin, to the PM. (A) MDCK cells were transfected with control RNA or Rab13 siRNA and subjected to Western blot analysis by using anti-Rab13 and anti-β-actin antibodies. The result shown is representative of three independent experiments. (B–D) MDCK cells transfected with control RNA or Rab13 siRNA were subjected to a Ca2+-switch assay and then immunostained with anti-claudin-1, anti-occludin, and anti-E-cadherin antibodies at the indicated time after Ca2+ restoration. Representative images of three independent experiments are shown. Bars, 20 µm. Claudin-1, occludin, and E-cadherin length is quantified and shown as the mean and SEM. The asterisks denote a significant difference between control RNA and Rab13 siRNA (p < 0.05).

View larger version (58K): [in this window] [in a new window]   Figure 2. JRAB/MICAL-L2 is involved in the transport of claudin-1, occludin, and E-cadherin to the PM. (A) MTD-1A cells were transfected with control RNA or JRAB/MICAL-L2 siRNA and subjected to Western blot analysis by using anti-JRAB/MICAL-L2 and anti-β-actin antibodies. The result shown is representative of three independent experiments. (B–D) MTD-1A cells transfected with control RNA or JRAB/MICAL-L2 siRNA were subjected to a Ca2+-switch assay and then immunostained with anti-claudin-1, anti-occludin, and anti-E-cadherin antibodies at the indicated time after Ca2+ restoration. Representative images of three independent experiments are shown. Bars, 20 µm. Claudin-1, occludin, and E-cadherin length is quantified and shown as the mean and SEM. The asterisks denote a significant difference between control RNA and JRAB/MICAL-L2 siRNA (p < 0.05).

View larger version (54K): [in this window] [in a new window]   Figure 3. Expression of the Rab13-binding domain of JRAB/MICAL-L2 inhibits the transport of claudin-1, occludin, and E-cadherin to the PM. (A) The Rab13-binding domain of JRAB/MICAL-L2. CH, calponin homology domain; LIM, LIM domain; and CC, coiled-coil domain. (B–D) MTD-1A cells infected with Ad-EGFP (GFP) or Ad-Myc-JRAB/MICAL-L2-C (JRAB-C) were subjected to a Ca2+-switch assay, and then they were immunostained with anti-claudin-1, anti-occludin, and anti-E-cadherin antibodies at the indicated time after Ca2+ restoration. Representative images of three independent experiments are shown. Bars, 20 µm. Claudin-1, occludin, and E-cadherin length is quantified and shown as the mean and SEM. The asterisks denote a significant difference between GFP and JRAB/MICAL-L2-C (p < 0.05).

View larger version (55K): [in this window] [in a new window]   Figure 4. Rab8A is identified as another JRAB/MICAL-L2-binding protein that mediates the Rab13-independent transport of E-cadherin to the PM. (A) Yeast transformants carrying the bait vector (pGBDU or pGBDU-JRAB/MICAL-L2-C) and the prey vector (pACT2 or pACT2-Rab8A) were spotted on synthetic complete medium containing or lacking adenine to score for ADE2 reporter activity, and then they were incubated at 30°C for 3 d. (B) BHK cells expressing Myc-JRAB/MICAL-L2-F with HA-Rab8A were immunoprecipitated (IP) in the presence of either GTPS (GTP) or GDP with an anti-HA antibody and subjected to Western blot (WB) analysis by using anti-Myc and anti-HA antibodies. The arrow indicates Myc-JRAB/ MICAL-L2-F, and the asterisk indicates a nonspecific band. (C) BHK cells expressing Myc-JRAB/MICAL-L2 with HA-Rab1A, HA-Rab3B, HA-Rab5A, HA-Rab8A, HA-Rab8B, HA-Rab10, or HA-Rab13 were immunoprecipitated with an anti-HA antibody and subjected to Western blot analysis by using anti-Myc and anti-HA antibodies. The arrow indicates Myc-JRAB/MICAL-L2-F, and the asterisk indicates the nonspecific band. (D) MTD-1A cells expressing HA-Rab4A, HA-Rab8A, HA-Rab11A, or HA-Rab13 were immunoprecipitated with an anti-HA antibody and subjected to Western blot analysis by using anti-JRAB/MICAL-L2 and anti-HA antibodies. The results shown in A–D are representative of three independent experiments. (E) MDCK cells transfected with control RNA or Rab8A siRNA were subjected to a Ca2+-switch assay, and then they were immunostained with an anti-E-cadherin antibody at the indicated time after Ca2+ restoration. Representative images of three independent experiments are shown. Bar, 20 µm. E-cadherin length is quantified and shown as the mean and SEM. The asterisks denote a significant difference between control RNA and Rab8A siRNA (p < 0.05).

If JRAB/MICAL-L2 mediated the Rab13-independent transport of E-cadherin to the PM and also interacted with Rab8A, Rab8A was possibly involved. To test this possibility, we designed three siRNAs targeting the canine Rab8A sequence (NM_001003152). Although all Rab8A siRNAs suppressed the expression of Rab8A protein in MDCK cells relative to a nonsilencing control RNA, the Rab8A-3 siRNA was the most effective and used in the present study (Supplemental Figure S4B). When we examined the transport of E-cadherin to the PM during the Ca²⁺ switch in control and Rab8A-depleted MDCK cells, it was substantially delayed in Rab8A-depleted cells relative to control cells (Figure 4E and Supplemental Figure S4C).

MICAL Family Proteins Specifically Interacts with Rab Family Proteins
Because JRAB/MICAL-L2 is a member of MICAL family proteins that is conserved from flies to mammals, with two MICAL family genes (D-MICAL and D-MICAL-L) identified in Drosophila and five (MICAL-1, MICAL-2, MICAL-3, MICAL-L1, and JRAB/MICAL-L2) found in mammals (Figure 5A) (Suzuki et al., 2002; Terman et al., 2002), we further investigated the interaction of Rab8A and Rab13 with other MICAL family proteins. HA-Rab8A or HA-Rab13 was coexpressed with Myc-MICAL-1, Myc-MICAL-2, Myc-MICAL-3, Myc-MICAL-L1, or Myc-JRAB/MICAL-L2 in BHK cells and analyzed by coimmunoprecipitation. Although HA-Rab8A precipitated with Myc-MICAL-1, Myc-MICAL-L1, and Myc-JRAB/MICAL-L2 but not with Myc-MICAL-2 and Myc-MICAL-3, HA-Rab13 preferentially interacted with Myc-JRAB/MICAL-L2 (Figure 5, B and C). To explore the physiological significance of these interactions, we next examined the role of MICAL-1, MICAL-L1, and JRAB/MICAL-L2 on the development of TER, which is often used to monitor the tightness of the seal created by functional TJs. For this purpose, we designed siRNAs targeting canine MICAL-1 (XM_539079 [GenBank] ), MICAL-L1 (XM_538381 [GenBank] ), and JRAB/MICAL-L2 (XM_547017 [GenBank] ), and we monitored their effect by quantitative real-time RT-PCR. MICAL-1, MICAL-L1, and JRAB/MICAL-L2 siRNAs efficiently suppressed the mRNA expression compared with a nonsilencing control RNA, and were used in the present study (Figure 5D). When cultured on permeable filters for 72–96 h, all MDCK I cells transfected with control RNA, MICAL-1 siRNA, MICAL-L1 siRNA, and JRAB/MICAL-L2 siRNA showed the high TER value (>800 cm²). However, these cells differed in the kinetics of TER development during a Ca²⁺-switch assay. Consistent with our previous observations in MTD-1A cells (Terai et al., 2006), the development of TER after 6 and 12 h of Ca²⁺ restoration was impaired in JRAB/MICAL-L2–depleted MDCK I cells compared with control cells (Figure 5E). Although we cannot formally exclude the involvement of MICAL-1 and MICAL-L1 at present, these results suggest that JRAB/MICAL-L2 is a key MICAL family member in the assembly of functional TJs.

View larger version (46K): [in this window] [in a new window]   Figure 5. MICAL family proteins specifically interact with Rab family proteins. (A) Structures of MICAL family proteins. FAD, FAD-binding domain; CH, calponin homology domain; LIM, LIM domain; and CC, coiled-coil domain. (B and C) BHK cells expressing Myc-MICAL-1, Myc-MICAL-2, Myc-MICAL-3, Myc-MICAL-L1, or Myc-JRAB/MICAL-L2 with HA-Rab8A (B) or HA-Rab13 (C) were IP with an anti-HA antibody and subjected to WB analysis by using anti-Myc and anti-HA antibodies. The arrows indicate Myc- MICAL-1, Myc-MICAL-L1, and Myc-JRAB/MICAL-L2, and the asterisks indicate nonspecific bands. The results shown in B and C are representative of three independent experiments. (D) Total RNA was prepared from MDCK I cells transfected with control RNA, MICAL-1 siRNA, MICAL-L1 siRNA, or JRAB/MICAL-L2 siRNA, and the relative mRNA expression of MICAL-1, MICAL-L1, and JRAB/MICAL-L2 to GAPDH was determined by quantitative real-time PCR analysis. Data were shown as the mean and SEM for triplicate determinations. The mean expression of MICAL-1, MICAL-L1, and JRAB/MICAL-L2 mRNA in MDCK I cells transfected with control RNA was set to 1. (E) MDCK I cells transfected with control RNA, MICAL-1 siRNA, MICAL-L1 siRNA, and JRAB/ MICAL-L2 siRNA were subjected to Ca2+-switch assay. TER was measured at 6 and 12 h after Ca2+ restoration. The results shown are the mean and SEM of three independent experiments.

View larger version (57K): [in this window] [in a new window]   Figure 6. Rab8 competes with Rab13 for the binding to JRAB/MICAL-L2. (A) Structures of JRAB/MICAL-L2-C, JRAB/MICAL-L2-CC, and JRAB/MICAL-L2-CT proteins. CH, calponin homology domain; LIM, LIM domain; and CC, coiled-coil domain. (B) BHK cells expressing Myc-JRAB/MICAL-L2-C, Myc-JRAB/MICAL-L2-CC, or Myc-JRAB/MICAL-L2-CT with HA-Rab8A or HA-Rab13 were IP with an anti-HA antibody and subjected to WB analysis by using anti-Myc and anti-HA antibodies. The arrow indicates Myc-JRAB/MICAL-L2-C, and the asterisks indicate nonspecific bands. (C) BHK cells cotransfected with pCI-neo-HA-JRAB/MICAL-L2 (+, 2.0 µg) and pCI-neo-Myc-Rab13 (+, 1.0 µg) together with pCI-neo-Myc (–, 2.0 µg), pCI-neo-Myc + pCI-neo-Myc-Rab8A (+, 1.5 + 0.5 µg), or pCI-neo-Myc-Rab8A (++, 2.0 µg) were IP with an anti-HA antibody and subjected to WB analysis by using anti-Rab13, anti-Rab8, and anti-JRAB/MICAL-L2 antibodies. (D) BHK cells cotransfected with pCI-neo-HA-JRAB/MICAL-L2 (+, 2.0 µg) and pCI-neo-Myc-Rab8A (+, 1.0 µg) together with pCI-neo-Myc (–, 2.0 µg), pCI-neo-Myc + pCI-neo-Myc-Rab13 (+, 1.5 + 0.5 µg), or pCI-neo-Myc-Rab13 (++, 2.0 µg) were IP and subjected to WB analysis as described in C. The results shown in B–D are representative of three independent experiments.

JRAB/MICAL-L2 Interacts with Rab8 and Rab13 at Specific Intracellular Sites
We then analyzed the intracellular localization of Rab8, Rab13, and JRAB/MICAL-L2 in MDCK cells. In agreement with previous reports (Huber et al., 1993b; Marzesco et al., 2002; Ang et al., 2004; Terai et al., 2006), Rab8A, Rab13, and JRAB/MICAL-L2 were all detected at perinuclear membrane structures, vesicular structures in the cytosol, and PM (Figure 7, A and B). To characterize the intracellular sites where JRAB/MICAL-L2 interacted with Rab8A and Rab13, FLAG-tagged Rab8A (FLAG-Rab8A) or FLAG-tagged Rab13 (FLAG-Rab13) was coexpressed with HA-JRAB/MICAL-L2 and colabeled with markers for the Golgi (Golgi 58K), the early endosome (EEA1), the late endosome (M6PR), the recycling endosome (Alexa-Tf), and the PM (ZO-1). Although FLAG-Rab8A colocalized with HA-JRAB/MICAL-L2 at the sites labeled with the internalized Alexa-Tf, Golgi 58K, and ZO-1, a closer spatial relationship between FLAG-Rab8A, HA-JRAB/MICAL-L2, and the internalized Alexa-Tf was observed (Figure 7A). Similarly, FLAG-Rab13, HA-JRAB/MICAL-L2, and ZO-1 showed a closer spatial relationship, albeit FLAG-Rab13 also associated with HA-JRAB/MICAL-L2 at the internalized Alexa-Tf and Golgi 58K-positive sites (Figure 7B). To further define the interaction sites of JRAB/MICAL-L2 with Rab8A and Rab13, HA-JRAB/MICAL-L2 was coexpressed with a GTP hydrolysis-defective mutant of FLAG-Rab8A (FLAG-Rab8A Q67L) or FLAG-Rab13 (FLAG-Rab13 Q67L) in MDCK cells. Although an intracellular distribution pattern of FLAG-Rab8A Q67L and FLAG-Rab13 Q67L was very similar to that of FLAG-Rab8A and FLAG-Rab13, the distinct localization of Rab8A-JRAB/MICAL-L2 and Rab13-JRAB/MICAL-L2 complexes was frequently emphasized in the presence of FLAG-Rab8A Q67L and FLAG-Rab13 Q67L (Figure 7, C and D).

View larger version (88K): [in this window] [in a new window]   Figure 7. JRAB/MICAL-L2 interacts with Rab8 and Rab13 at specific intracellular sites. (A and B) MDCK cells coexpressing HA-JRAB/MICAL-L2 with FLAG-Rab8A (A) or FLAG-Rab13 (B) were triple labeled with anti-FLAG antibody, anti-HA antibody, and organella markers (anti-EEA1 antibody, anti-M6PR antibody, Alexa-Tf, anti-Golgi 58K antibody, and anti-ZO-1 antibody). Magnified images in inserts show the notable colocalization with organella markers. Bars, 20 µm. (C and D) MDCK cells coexpressing HA-JRAB/MICAL-L2 with FLAG-Rab8A Q67L (C) or FLAG-Rab13 Q67L (D) were double labeled with anti-FLAG and anti-HA antibodies. In the merged images, Rab8A Q67L/Rab13 Q67L was green and JRAB was red. The arrowheads indicate the sites of prominent colocalization. Bars, 20 µm. The results shown in A–D are representative of three independent experiments.

View larger version (57K): [in this window] [in a new window]   Figure 8. Rab8-JRAB/MICAL-L2 and Rab13-JRAB/MICAL-L2 complexes are involved in the recycling of E-cadherin and occludin to the PM. (A) MDCK cells labeled with Alexa-Tf were subjected to a Ca2+-switch assay in the presence of cycloheximide and then immunostained with anti-E-cadherin or anti-occludin antibody at the indicated time after Ca2+ restoration. The arrowheads indicate the overlap. Bar, 20 µm. (B) MDCK cells coexpressing HA-JRAB/MICAL-L2 with FLAG-Rab8A or FLAG-Rab13 were subjected to a Ca2+-switch assay in the presence of cycloheximide, and then they were triple labeled with anti-HA, anti-FLAG, and anti-E-cadherin or anti-occludin antibodies at 1 h after Ca2+ restoration. The arrows and arrowheads indicate the colocalization at the PM and PNC, respectively. Bar, 20 µm. (C–E) MDCK cells transfected with control RNA or JRAB/MICAL-L2 siRNA (C), pCI-neo-HA-JRAB/MICAL-L2 with control RNA or Rab8A siRNA (D), or pCI-neo-HA-JRAB/MICAL-L2 with control RNA or Rab13 siRNA (E) were subjected to a Ca2+-switch assay in the presence of cycloheximide and then immunostained with anti-E-cadherin, anti-occludin, and anti- HA antibodies at 1 h after Ca2+ restoration. E-cadherin or occludin length was quantified and shown as the mean and SEM. The asterisks denote a significant difference (p < 0.05). The ratio of JRAB/MICAL-L2-E-cadherin or JRAB/MICAL-L2-occludin colocalized area at the PNC to that at the PM was quantified and shown as the mean and SEM. The arrows and arrowheads indicate the colocalization at the PM and PNC, respectively. Bars, 20 µm. The images shown in A–E are representative of three independent experiments.

	DISCUSSION

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

 
The formation and destruction of TJs and AJs are essential for the physiological development of multicellular organisms. Failure in their regulation is manifested in a variety of diseases, such as tissue fibrosis and tumor invasion/metastasis. To gain insight into the molecular mechanisms of TJ and AJ assembly, we previously showed that Rab13 and JRAB/MICAL-L2 mediated the endocytic recycling of occludin and regulated the assembly of functional TJs (Morimoto et al., 2005; Terai et al., 2006). Our present study revealed five key findings. First, JRAB/MICAL-L2 regulated the transport of both TJ and AJ proteins to the PM, whereas Rab13 specifically mediated that of TJ but not AJ proteins. Second, JRAB/MICAL-L2 also interacted with Rab8, which mediated the Rab13-independent transport of AJ protein to the PM. Third, Rab8 and Rab13 competed with each other to bind JRAB/MICAL-L2. Fourth, JRAB/MICAL-L2 mainly associated with Rab8 and Rab13 at the PNC and PM, respectively. Fifth, depletion of Rab8 and Rab13 impaired the colocalization of JRAB/MICAL-L2 with AJ protein at the PNC and TJ protein at the PM, respectively. Collectively, these results suggest that JRAB/MICAL-L2 coordinates the assembly of AJ and TJ by forming the distinct Rab8-JRAB/MICAL-L2 and Rab13-JRAB/MICAL-L2 complexes (Figure 9).

View larger version (18K): [in this window] [in a new window]   Figure 9. Schematic model for the action of Rab8-JRAB/ MICAL-L2 and Rab13-JRAB/MICAL-L2 complexes in the assembly of AJs and TJs. Whereas the Rab8-JRAB/MICAL-L2 complex resided at the PNC mediates the recycling of E-cadherin to the PM and the assembly of AJs, the Rab13-JRAB/MICAL-L2 complex resided at the PM regulates the recycling of claudins and occludin to the PM and the formation of TJs. N, nucleus.

In the present study, we found that JRAB/MICAL-L2 controlled the transport of claudins, occludin, and E-cadherin to the PM, and Rab8 regulated the Rab13-independent transport of E-cadherin to the PM. Although knockdown of Rab8 also impaired the transport of claudins and occludin (Supplemental Figure S4, D and E), this could be caused by the inhibition of E-cadherin transport as TJ protein transport was depend on AJ protein transport in a Ca²⁺-switch model (Yap et al., 1997; Takai and Nakanishi, 2003). The present study adds JRAB/MICAL-L2 and Rab8 to a growing list of regulatory molecules for E-cadherin trafficking (Bryant and Stow, 2004; D'Souza-Schorey, 2005; Ivanov et al., 2005). Although Rab8 is functionally linked to epithelial specific clathrin adaptor complexes AP-1B and E-cadherin is initially recognized as an AP-1B-independent basolateral cargo (Miranda et al., 2001; Ang et al., 2003; Fölsch, 2005), a recent observation that phosphatidylinositol-4-phosphate 5-kinase modulates the basolateral transport of E-cadherin and directly binds both E-cadherin and AP-1B supports our results (Ling et al., 2007). Furthermore, Rab8 is recently shown to colocalize with Rab11 and ARF6, both of which are implicated in the transport of E-cadherin, and it is functionally linked to ARF6 (Palacios et al., 2001; Lock and Stow, 2005; Hattula et al., 2006). Collectively, Rab8, Rab11, and ARF6 seem to coordinate the transport of E-cadherin to the PM. Although the exact nature of this coordination remains elusive, one possible explanation would be that Rab8, Rab11, and ARF6 sequentially act through the same transport pathway of E-cadherin. In this scenario, a cascade of Rab8, Rab11, and ARF6 would be expected. Alternatively, Rab8, Rab11, and ARF6 could simultaneously work on the distinct transport pathways of E-cadherin. This case would predict the existence of different populations of transport carriers containing E-cadherin.

Then, the question of how JRAB/MICAL-L2 works as a shared Rab8 and Rab13 effector protein on the transport of E-cadherin and occludin to the PM has naturally arisen. As JRAB/MICAL-L2 is directly or indirectly associated with actin cytoskeletons (Terai et al., 2006), we speculate the involvement of JRAB/MICAL-L2 in the membrane-actin cytoskeleton interactions, and we can formulate several models to explain the present results. Considering a widespread concept that Rab and its effector proteins can recruit myosin motors onto the transport carrier membranes (Seabra and Coudrier, 2004), Rab8-JRAB/MICAL-L2 and Rab13-JRAB/MICAL-L2 complexes could recruit myosin motors onto the transport carrier membranes containing E-cadherin and occludin, respectively. Although we did not detect the colocalization of Rab8-JRAB/MICAL-L2 and Rab13-JRAB/MICAL-L2 on the transport carriers, we cannot formally exclude this model at the moment. Alternatively, Rab8-JRAB/MICAL-L2 and Rab13-JRAB/MICAL-L2 complexes could mediate the membrane-actin cytoskeleton interactions at the PNC and PM, respectively. According to this model, Rab8-JRAB/MICAL-L2 complex would sort E-cadherin within the PNC membranes or generate E-cadherin transport carrier from the PNC, whereas Rab13-JRAB/MICAL-L2 complex would tether/dock/fuse occludin transport carrier with the PM. JRAB/MICAL-L2 would directly mediate these processes or scaffold the executing molecule(s) as it contains multiple protein–protein interaction domains. The further determination of the JRAB/MICAL-L2-interacting molecules would be essential for this model.

Another important question is how JRAB/MICAL-L2 controls its interaction with Rab8 and Rab13. Although the intracellular distribution of Rab8, Rab13, and JRAB/MICAL-L2 were overlapped at the PNC and PM, the Rab8-JRAB/MICAL-L2 and Rab13-JRAB/MICAL-L2 interactions were preferentially detected at the PNC and PM, respectively. Because Rab8 and Rab13 compete with each other for the interaction with JRAB/MICAL-L2 (Figure 6, C and D), there must exist the additional mechanism(s) to activate/stabilize the Rab8-JRAB/MICAL-L2 and Rab13-JRAB/MICAL-L2 interactions at the PNC and PM, respectively. Alternatively, the Rab8-JRAB/ MICAL-L2 and Rab13-JRAB/MICAL-L2 interactions might be inactivated/prevented at the PM and PNC, respectively. In support of stabilizing mechanism for the Rab13-JRAB/MICAL-L2 interaction at the PM, JRAB/ MICAL-L2 also interacted with actinin-4 and made the Rab13-JRAB/MICAL-L2-actinin-4 complex at TJs (our unpublished observations). Other potential stabilizing and/or preventing mechanisms for the Rab8-JRAB/ MICAL-L2 and Rab13-JRAB/MICAL-L2 interactions are currently under investigation.

In accordance with the involvement of JRAB/MICAL-L2 in TJ and AJ assembly, a series of recent studies begin to reveal the potential role of MICAL family proteins in the regulation of invasive growth (Comoglio and Trusolino, 2002). MICAL-1, MICAL-2, and MICAL-3 are shown to function downstream of the Semaphorin 3 receptor Plexin A during axon guidance (Terman et al., 2002). The MICAL-2 isoforms (MICAL-2 PVa and PVb) are implicated in the progression of prostate cancer (Ashida et al., 2006). Consistent with the obligatory demand for extensive membrane trafficking and cytoskeletal rearrangement during invasive growth, the interactions of MICAL family proteins with Rab1, vimentin, and microtubules are also detected (Suzuki et al., 2002; Weide et al., 2003; Fischer et al., 2005).

In summary, our results suggest that JRAB/MICAL-L2 represents a novel type of a shared Rab effector protein that forms mutually distinct complexes with closely related Rab8 and Rab13. JRAB/MICAL-L2 interacts with the GTP-bound forms of Rab8 and Rab13 at the PNC and PM, respectively, and the Rab8-JRAB/MICAL-L2 and Rab13-JRAB/MICAL-L2 complexes coordinate the assembly of AJs and TJs through the regulation of Rab8-dependent E-cadherin transport and Rab13-dependent claudins/occludin transport.

	ACKNOWLEDGMENTS

 
We thank Dr. W. Birchmeier for the MDCK cells, Dr. T. Tsukamoto for the MDCK I cells, and Dr. S. Tsukita for the MTD-1A cells and the anti-occludin (MOC37) antibody. This study was supported by Grants-in-Aid for Scientific Research (18590271 to N.N. and 15079207, 18390089 to T.S.) from the Ministry of Education, Culture, Sports, Science and Technology of Japan.

	Footnotes

 
This was published online ahead of print in MBC in Press (http://www.molbiolcell.org/cgi/doi/10.1091/mbc.E07-06-0551) on December 19, 2007.

Address correspondence to: Takuya Sasaki (sasaki{at}basic.med.tokushima-u.ac.jp)

Abbreviations used: AJ, adherens junction; CC, coiled-coil; PM, plasma membrane; siRNA, small interfering RNA; TfR, transferrin receptor; TJ, tight junction; ZO, zonula occludens.

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